Evidence map›Paper›PMID 39678599›Full record

ArticleAmerican journal of translational research2024

Comprehensive analysis of the pituitary tumor-transforming gene (PTTG) family in lung adenocarcinoma: diagnostic, prognostic, and therapeutic implications.

Jiajia Xu, Xueping Lou, Fei Li, Biying Song, Yiting Zheng, Jie Zhu, Zhencang Zheng

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Article in American journal of translational research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Jiajia XuClinical Laboratory, Taizhou Central Hospital (Taizhou University Hospital) Taizhou 318000, Zhejiang, China.
Xueping LouOffice of Taizhou Enze Medical Center (Group) Enze Hospital Taizhou 318050, Zhejiang, China.
Fei LiClinical Laboratory, Taizhou Central Hospital (Taizhou University Hospital) Taizhou 318000, Zhejiang, China.
Biying SongClinical Laboratory, Taizhou Central Hospital (Taizhou University Hospital) Taizhou 318000, Zhejiang, China.
Yiting ZhengJiaojiang District Center for Disease Prevention and Control Taizhou 318000, Zhejiang, China.
Jie ZhuClinical Laboratory, Taizhou Central Hospital (Taizhou University Hospital) Taizhou 318000, Zhejiang, China.
Zhencang ZhengDepartment of Critical Care Medicine, Taizhou Central Hospital (Taizhou University Hospital) Taizhou 318000, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesLung adenocarcinoma (LUAD) is a prevalent form of non-small cell lung cancer with high morbidity and mortality rates. Identifying molecular markers and therapeutic targets is crucial for improving LUAD diagnosis and treatment. Pituitary tumor-transforming gene (PTTG) family members, PTTG1, PTTG2, and PTTG3P, have been linked to several malignancies; however, it is unclear how these genes relate to LUAD. The current retrospective study investigates the diagnostic, prognostic, and therapeutic importance of PTTG genes in LUAD.

methodsWe used detailed in silico and in vitro experiments involving cell lines for experimental design.

resultsUsing RT-qPCR, we documented that PTTG1, PTTG2, and PTTG3P are significantly up-regulated in LUAD cell lines compared to controls, with PTTG2 showing the highest diagnostic potential (AUC = 1.0). Promoter methylation analysis revealed hypomethylation in LUAD samples, particularly for PTTG3P, further supporting its diagnostic relevance. Immunohistochemical staining confirmed overexpression of PTTG1 and PTTG2 proteins in LUAD tissue samples. The mutational analysis highlighted PTTG2 as the most frequently mutated gene within the PTTG family in LUAD samples, with mutations primarily being missense types. Survival analysis demonstrated that high expression of PTTG genes is associated with poorer overall survival, indicating their prognostic value. Gene enrichment analysis suggested that PTTG genes are involved in critical cancer-related pathways and cellular processes. Functional assays following siRNA-mediated knockdown of PTTG genes in A549 cells showed a significant reduction in cell proliferation. Lastly, drug sensitivity analysis revealed strong correlations between PTTG1/PTTG3P expression and resistance to various anticancer drugs.

conclusionThe findings of the current study highlight the potential of PTTG genes as diagnostic biomarkers, prognostic indicators, and therapeutic targets in LUAD.

Indexed as

biomarkerLUADPTTG family genestherapeutic target

Identifiers

PMID39678599
PMCPMC11645599

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.